hypertrophic cardiomyopathy 17 (Q27674936)
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hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the junctophilin gene (JPH2) on chromosome 20q12
- CMH17
- cardiomyopathy familial hypertrophic 17
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17; CMH17
- hypertrophic cardiomyopathy type 17
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17
- Cardiomyopathy, Familial Hypertrophic, type 17
- familial hypertrophic cardiomyopathy type 17
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hypertrophic cardiomyopathy 17 |
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the junctophilin gene (JPH2) on chromosome 20q12 |
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Statements
1 reference
2 references
C172093
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Identifiers
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1 reference